2024年12月25日 · LBR (Lamin B Receptor) is a Protein Coding gene. Diseases associated with LBR include Greenberg Dysplasia and Rhizomelic Skeletal Dysplasia With Or Without Pelger …

Lamin-B receptor is a protein, and in humans, it is encoded by the LBR gene. [5][6][7] The protein encoded by this gene belongs to the ERG4 / ERG24 family. It localizes to the inner membrane …

The LBR gene provides instructions for making a protein called the lamin B receptor. Different regions (domains) of this protein give it two distinct functions.

Lamin B receptor (LBR) is an integral protein of the inner nuclear membrane, containing a hydrophilic N -terminal end protruding into the nucleoplasm, eight hydrophobic segments that …

2022年2月23日 · A homozygous variant in the Lamin B receptor gene LBR results in a non-lethal skeletal dysplasia without Pelger-Huet anomaly.

Lamin B receptor (LBR) is an integral membrane protein of the interphase nuclear envelope (NE). The N-terminal end resides in the nucleoplasm, binding to lamin B and heterochromatin, with …

The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. …

Lamin B receptor (LBR) is a polytopic membrane protein residing in the inner nuclear membrane in association with the nuclear lamina. We demonstrate that human LBR is essential for …

A homozygous variant in the Lamin B receptor gene LBR results in a non-lethal skeletal dysplasia without Pelger-Huet anomaly. The role of lamin B receptor in the regulation of senescence …

The LBR gene encodes the lamin B receptor, an inner nuclear membrane protein that binds lamin B (LMNB1; 150340 and LMNB2; 150341). The nuclear envelope is composed of the nuclear …